|Publication number||US5460837 A|
|Application number||US 08/233,554|
|Publication date||Oct 24, 1995|
|Filing date||Apr 26, 1994|
|Priority date||Apr 16, 1991|
|Also published as||EP0523316A1|
|Publication number||08233554, 233554, US 5460837 A, US 5460837A, US-A-5460837, US5460837 A, US5460837A|
|Inventors||Nicola D'Amico, Thang H. Dac, Tomaso Sozzi, Robert D. Wood|
|Original Assignee||Nestec S.A.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (7), Non-Patent Citations (10), Referenced by (4), Classifications (16), Legal Events (4)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a continuation application of application Ser. No. 07/850,093, filed Mar. 12, 1992, and now abandoned.
This invention relates to a process for the production of a malolactic ferment, to the ferment thus obtained and to its use in the production of a wine.
There are various processes for deacidifying wine by malolactic fermentation during which malolactic bacteria, more particularly Leuconostoc oenos and certain lactobacilli, convert the malic acid present in the wine into lactic acid.
U.S. Pat. No. 4,380,552, for example, proposes deacidifying a wine by passing it through a bed of gel beads containing viable cells of Leuconostoc oenos . However, it is not certain that this process is any better than direct inoculation of the wine with this bacterium.
In European Patent Application Publication No. 327 380, wine is subjected to controlled malolactic fermentation by passage through a vessel containing at least 108 cells of malolactic bacteria per ml and delimited upstream and downstream by filters which retain the bacteria. The same batch of bacteria could be used for a relatively long time in continuous operation or for up to 5 or 6 months by carrying out fermentation in batches. However, both the process and the equipment used appear relatively complicated.
U.S. Pat. No. 4,562,077 proposes reducing the malic acid content of a wine by converting this acid into lactic acid using frozen or freeze-dried ferments containing strains of Leuconostoc oenos selected for their good activity in a quantity of 108 to 1013 cells/ml. However, the proposed ferments have to be specially activated before the wine can be inoculated with them.
U.S. Pat. No. 4,547,373 proposes strains of Leuconostoc oenos capable of achieving relatively rapid malolactic fermentation, namely in about 50 to 100 d, for example at a relatively low temperature of approximately 16° to 18° C. and at a relatively low pH value of about 3.1 to 3.2.
In addition, there are commercially available malolactic ferments intended for use in traditional vinification when it is desired to exercise better control over the malolactic fermentation of a must or a wine rich in malic acid. However, almost all these commercial ferments have to be reactivated before use, for example over a period of two days on a particular medium, which complicates the task of the cellarman.
There are also various processes for making so-called light wines, i.e. wines of which the alcohol content is substantially reduced in relation to that of a so-called normal wine which has an alcohol content of approximately 8.5 to 16% by volume (8.5° to 16° alcohol).
U.S. Pat. No. 4,626,437, for example, describes a process for making a light wine in which a normal wine is subjected to an evaporation process to remove alcohol and aromatic constituents, leaving a condensate which is then subjected to fractional distillation to remove an aromatic fraction and the aromatic fraction thus obtained is returned to the wine reduced in alcohol and aromatic constituents. Unfortunately, a light wine made in this way can still have a substantially modified flavour in relation to that of the starting wine.
U.S. Pat. No. 4,902,518 describes a process for making a light wine in which grape juice is separated into a fraction rich in sugar and a fraction poor in sugar, an aromatic fraction is recovered from the fraction rich in sugar and is added to the fraction poor in sugar which is then subjected to traditional fermentation. A light wine made in this way can differ considerably in its flavour from a wine obtained by traditional fermentation of the starting grape juice.
Since the flavour of a wine is significantly influenced or even strengthened by malolactic fermentation during or after alcoholic fermentation, it could be of advantage to subject light wines of the type in question to malolactic fermentation during or after their production. However, this would presuppose control of the malolactic fermentation process.
Accordingly, there is a need for a reliable and effective malolactic ferment which would be capable of initiating and then rapidly completing malolactic fermentation on direct inoculation into a normal or light wine.
The object of the present invention is to obviate the disadvantages of known deacidification processes and known ferments and to satisfy the need mentioned above for a reliable and effective malolactic ferment so that the production of normal or light wines could be improved.
To this end, the process according to the invention for the production of a malolactic ferment is characterized in that a culture medium containing alcohol, an assimilable nitrogen source and malic acid is prepared, a biomass is prepared by inoculation and culture of at least one strain of malolactic bacterium in the culture medium and the biomass is then separated.
It has surprisingly been found that a ferment prepared in this way can effectively be inoculated directly into a wine in which it immediately initiates vigorous and rapid malolactic fermentation in a reliable and effective manner.
To carry out the process according to the invention, the alcohol-containing culture medium may be prepared by alcoholic fermentation of a base medium containing a fermentable sugar, more particularly a fruit juice or an approximately 5 to 15% by weight solution of sucrose, glucose or fructose for example, this juice or this solution additionally containing the assimilable nitrogen source and the malic acid. The alcoholic fermentation process may be carried out using any yeast known for producing alcohol, more particularly yeasts of the type used in oenology and, more particularly, yeasts of the species Saccharomyces cerevisiae for example. The base medium may be inoculated at ambient temperature with approximately 1 to 5% by volume of a traditional ferment or with approximately 0.02 to 0.1% by weight of a commercial concentrated ferment of S. cerevisiae and then left to ferment, for example for about 1 to 4 d. Since the pH of the base medium is approximately 2.8 to 3.2 after fermentation under these conditions, it may then be adjusted, if necessary, to approximately pH 3-4.5 and preferably to pH 3.4-3.6, for example by addition of a concentrated NaOH solution.
The alcohol-containing culture medium may also be prepared by directly mixing alcohol and water so that the resulting mixture has an alcohol content of approximately 2.5 to 8% by volume for example. This mixture may also contain the assimilable nitrogen source and the malic acid. If the culture medium is prepared in this way, its pH value may also be adjusted to pH 3-4.5 and preferably to pH 3.4-3.6.
Various materials rich in amino acids or polypeptides, such as a yeast extract, a vegetable or animal protein hydrolyzate, a corn steep liquor or ammonium citrate may be used as the assimilable nitrogen source in the culture medium, for example in a quantity of 0.1 to 1% by weight.
The malic acid may be incorporated in the culture medium in a quantity of approximately 0.1 to 2% by weight for example.
It is also possible to add to the culture medium approximately 0.05 to 0.5% by weight glucose in order, if necessary, to facilitate growth of the malolactic bacterium and approximately 1 to 10 mg/l SO2, for example in the form of sodium bisulfite, to induce a resistance of the malolactic bacterium to SO2 or, more precisely, to the H2 SO3 which is formed in the medium as a result of this addition.
The culture medium may be inoculated with approximately 0.5 to 5% of a culture containing approximately 107 to 109 cells of at least one strain of malolactic bacterium per ml. This/these strain(s) may be selected from strains of lactic bacteria which are capable of effecting the malolactic fermentation and of producing an agreeable flavour, such as for example strains of Leuconostoc oenos, Lactobacillus brevis or Lactobacillus plantarum. This/these strain(s) is preferably selected from strains of Leuconostoc oenos which may be isolated from wines undergoing their malolactic fermentation in the cellars of wine growers of central Europe and, more particularly, Switzerland for example. Four strains from which a ferment of particularly remarkable quality can be prepared have been selected from numerous preferred strains thus isolated. These four strains of Leuconostoc oenos were lodged by way of example in the Collection Nationale de Cultures de Microorganismes (CNCM), Institut Pasteur, 28 rue du Dr Roux, 7524 Paris Cedex 15, France, on the 29.03.91 under the Budapest Treaty and have been given the Nos. CNCM I-1063, I-1064, I-1065 and I-1066. These four strains are very similar to one another and, essentially, are only distinguished from one another by their different sensitivity to phages. Particulars of their morphology and their properties are given in the following.
Gram-positive microorganism, negative catalase and optional anaerobe.
Small spherical cells, occasionally lenticular, in more or less long chains (on MRS medium).
The cells may be elongated or may even be in the form of bacilli on wine (particularly acid wine, pH 3.0-3.2).
No presence of flagellae, no spore formation.
Fermentation of sugars:
Production of acid from glucose.
Ability to ferment the malate into L(+) lactic acid in the presence of alcohol (malolactic fermentation)
CNCM I-1063, I-1065 and I-1066
The morphology and properties of each of these strains are the same as those described above for the strain CNCM I-1064.
The said lactic bacterium strain can be cultivated in the said culture medium at ambient temperature, in other words at a temperature of around 18° to 30° C., over a period of about 1 to 4 d until the medium contains approximately 107 to 109 cells/ml.
The biomass thus obtained may then be separated and, if necessary, concentrated approximately 20 to 100 times, for example by ultrafiltration or centrifugation.
After it has been separated and, if necessary concentrated, the biomass may be dehydrated, more particularly by freeze-drying for example. In a preferred embodiment, it is frozen after the addition of a cryoprotective agent, such as glycerol for example, and after pH adjustment to approximately 4.2 to 4.8.
The malolactic ferment thus obtained may contain approximately 5.108 to 101l cells/g. It may be used for converting malic acid into lactic acid during the production of a wine. It is distinguished by its ability to initiate malolactic fermentation on direct inoculation into a wine and is capable of rapidly completing this fermentation process.
In addition to the use of the ferment in the production of a so-called normal wine, the present invention also relates to its use in the production of a so-called light wine.
Thus, the present invention relates more particularly to the use of the ferment according to the invention in a first particular process for the production of a light wine comprising partial separation of sugar from a grape must, more particularly by ultrafiltration, alcoholic fermentation of the sugar-reduced must and malolactic fermentation of the low-alcohol wine thus obtained.
The present invention also relates to the use of the ferment according to the invention in a second particular process for the production of a light wine comprising at least partial alcoholic fermentation of a grape must, at least partial elimination of the alcohol produced during this alcoholic fermentation and malolactic fermentation and/or secondary alcoholic fermentation of the low-alcohol wine thus obtained.
For these uses, the ferment according to the invention may be directly inoculated in a quantity of approximately 0.01 to 0.1% by weight into a wine at approximately 18° to 30° C. which has a total SO2 content below about 50 mg/l and a suitable pH, depending on its alcohol content. For a so-called normal wine having an alcohol content of approximately 8.5 to 16% by volume, this suitable pH may be approximately 3.1 to 4.5. For a so-called light wine having an alcohol content of approximately 0.5 to 8.5% by volume, this suitable pH may be approximately 2.6 to 4.0.
The process for the production and the uses of the malolactic ferment according to the invention are illustrated by the following Examples in which percentages and parts are by weight, unless otherwise indicated.
A base medium is prepared in the form of an aqueous 10% solution of sucrose additionally containing 0.5% yeast extract, 0.5% corn steep liquor and 0.5% malic acid. This base medium is inoculated with 2% by volume of a commercial wine-making yeast of Saccharomyces cerevisiae and is then left to ferment for 3 d at ambient temperature.
A culture medium having an alcohol content of 6.2% by volume and a pH of 3.1 is thus obtained, its pH being adjusted to 3.4 by addition of a 20% aqueous NaOH solution. 3 mg/l SO2 in the form of sodium bisulfite and 0.1% glucose are then added.
The culture medium is then inoculated with 3% by volume of a culture containing approximately 107 cells/ml of each of the Leuconostoc oenos strains CNCM I-1063, I-1064, I-1065 and I-1066. These strains are cultured in the medium for 3 d at ambient temperature. The biomass of Leuconostoc oenos thus obtained is then separated by centrifugation. It is resuspended in a cryoprotective aqueous medium containing 10% glycerol and its pH is adjusted to 4.5. A malolactic ferment is obtained of which the volume is reduced by a factor of 50 in relation to the culture medium and which contains approximately 2.109 cells/ml.
This ferment is frozen by spraying into liquid nitrogen. A frozen ferment is thus obtained in the form of ready-to-use beads containing approximately 2.109 cells of Leuconostoc oenos per g.
After alcoholic fermentation of a must sulfited with 40 mg SO2 /l, a Chasselas wine has an alcohol content of 11.4% by volume, a pH value of 3.39, a tartaric acid content of 3.3 g/l, a malic acid content of 3.2 g/l and a total SO2 content of 10 mg/l.
This wine is inoculated in a 100 l tank with 0.02% by weight frozen beads of the malolactic ferment obtained in Example 1. The development of this inoculated wine is followed in relation to that of the same, but non-inoculated wine in a 100 1 tank (for comparison).
A reduction in the malic acid content of the inoculated wine from 3.2 to 2.5 g/l is observed in the first week, from 2.5 to 1.2 g/l in the second week and from 1.2 g/l to virtually 0 g/l between the fourteenth and twenty-third days.
By contrast, it takes about 40 d for the malic acid content of the non-inoculated wine to fall to substantially g/l, the real start of the malolactic fermentation process being delayed by almost 20 d in relation to that of the inoculated wine.
On completion of malolactic fermentation, i.e., after 23 d and 40 d, respectively, the inoculated wine and the non-inoculated wine each contain more than 107 Leuconostoc oenos cells per ml. Accordingly, they are as good as one another.
A Gamay must was sulfited with 75 mg SO2 /l. Its alcoholic fermentation is initiated 5 h later by inoculation with 0.04% by weight of a reactivated suspension of commercial dehydrated yeast of Saccharomyces cerevisiae. Fermentation is left to continue for 2 to 3 d at 21° to 29° C. Fermentation is interrupted when the alcohol content reaches 7% by volume.
The pulp is separated for pressing and the partly fermented wine thus obtained is subjected to distillation in vacuo during which volatile aromas are first recovered, after which its alcohol content is reduced to approximately 4 to 5% by volume. The aromas recovered are then returned to the low-alcohol wine thus obtained. In addition, this wine has a pH value of 3.23 and a negligible total SO2 content.
The wine is cooled to 18° C. and inoculated with 1% by volume of a commercial yeast of Saccharomyces cerevisiae and with 0.1% by weight of frozen beads of the Leuconostoc oenos ferment obtained in Example 1. Malolactic fermentation and secondary alcoholic fermentation are allowed to take place at the same time over a period of 12 d at 18° to 20° C.
The light wine obtained in this way has an alcohol content of 8.2% by volume, a residual malic acid content of substantially zero and an agreeable wine flavour.
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|Citing Patent||Filing date||Publication date||Applicant||Title|
|US7112346||Mar 3, 1997||Sep 26, 2006||Chr. Hansen A/S||Method of inducing malolactic fermentation in wine or fruit juice by direct inoculation with a non-activated started culture|
|US7892583||Jun 25, 2004||Feb 22, 2011||Chr. Hansen A/S||Initiation of fermentation|
|EP2233559A1||Jun 25, 2004||Sep 29, 2010||Chr. Hansen A/S||Initiation of Fermentation|
|WO2004113488A2 *||Jun 25, 2004||Dec 29, 2004||Vinobios Aps||Initiation of fermentation|
|U.S. Classification||426/11, 426/15, 426/14, 426/592|
|International Classification||C12G1/10, C12G1/022, C12H1/00, C12P7/56|
|Cooperative Classification||C12P7/56, C12G1/0203, C12R1/01, C12H1/006|
|European Classification||C12G1/02B, C12H1/00B2, C12P7/56, C12R1/01|
|Oct 1, 1996||CC||Certificate of correction|
|May 18, 1999||REMI||Maintenance fee reminder mailed|
|Oct 24, 1999||LAPS||Lapse for failure to pay maintenance fees|
|Jan 4, 2000||FP||Expired due to failure to pay maintenance fee|
Effective date: 19991024